Purpose
Exposure Monitoring
Method(s)
Colorimetry (C)
Inductively Coupled Plasma/Mass Spectrometry (ICP/MS)
Suggested CPT Code(s)
82570
83789
New York State Approval Status

Approved

Turnaround Time

8 days (If Positive: 12 days)

Test Includes
1 Creatinine Colorimetry (C) mg/L 100 Biological Marker (Renal)
2 Iodine Inductively Coupled Plasma/Mass Spectrometry (ICP/MS) mcg/L 20 Non-Metal, Halogenide
3 Iodine (Creatinine corrected) Inductively Coupled Plasma/Mass Spectrometry (ICP/MS) mcg/g Creat

Reflex Tests
Test Code Test Name
6022U Specific Gravity Confirmation, Urine
Specimen Type
Urine
Requested Volume
3 mL
Minimum Volume
1.4 mL
Special Handling
None
Specimen Container
Plastic container (Trace metal-free rinsed with deionized water), Plastic container (preservative-free)

Additional Collection Instructions

Transport Temperature
Refrigerated
Light Protection
Not Required
Rejection Criteria
Received Room Temperature. Gray top tube (Sodium Fluoride / Potassium Oxalate), Lavender top tube (EDTA).

Rejection criteria pertain to clinical specimen submissions only.

Stability
Room Temperature: 5 day(s)
Refrigerated: 30 day(s)
Frozen (-20 °C): 30 day(s)
1 Creatinine Colorimetry (C) mg/L 100 Biological Marker (Renal)
2 Iodine Inductively Coupled Plasma/Mass Spectrometry (ICP/MS) mcg/L 20 Non-Metal, Halogenide
3 Iodine (Creatinine corrected) Inductively Coupled Plasma/Mass Spectrometry (ICP/MS) mcg/g Creat

Interface Map

LOINC® Information